Joint first authors.
University of Oxford.
Milbank Q. 2020 Jun;98(2):581-617. doi: 10.1111/1468-0009.12455. Epub 2020 May 20.
Policy Points For complex reasons, the promise of "precision medicine" based on molecular pathways remains unrealized for many conditions. Clinical practice guidelines (theoretically, at least) can act as "trailblazers" to introduce tests and treatments that reflect precision medicine discoveries. We describe a detailed case study from the United Kingdom in which such an attempt was (so far) unsuccessful and show how this case provides generalizable lessons. Policymakers should be wary of using clinical practice guidelines as the sole, or even the primary, lever for introducing precision medicine.
Precision medicine, which addresses underlying molecular mechanisms of disease, depends on new technologies that measure specific biomarkers, leading (it is anticipated) to more accurate diagnosis, patient stratification, and tailored treatment. These technologies can be disruptive-that is, they make possible, and often require, radical changes to clinical practice and service organization-thereby improving quality, safety, or efficiency of care. Clinical practice guidelines may act as "trailblazers," introducing and legitimizing novel technologies and practices.
We describe a case study of an attempt by academic researchers to radically change asthma management in the United Kingdom using a precision medicine biomarker (fractional exhaled nitric oxide, FeNO), measured using a portable breath device. We collected a wide-ranging data set that included more than 100 documents, 61 interviews, and 150 hours of ethnographic observation, and we analyzed it using technology-enhanced strong structuration theory (TESST).
Our study describes a so-far unsuccessful attempt by academic respiratory medicine researchers to pave the way for a precision medicine approach to asthma using a government-endorsed national guideline. These researchers considered asthma management, especially in primary care, to be characterized by overdiagnosis and poor tailoring of treatment; engaged a national guideline development body in an effort to fix this problem; and ensured that the guideline required primary care clinicians to use FeNO technology for diagnosis and monitoring. However, clinicians working outside the tertiary referral centers did not accept, or agree to enact, the vision of precision medicine inscribed in the guideline-for multiple professional, operational, and economic reasons.
"Trailblazer" guidelines, in which new technologies are recommended, may succeed as catalysts of change only in a limited way for interested individuals and groups. In the absence of a wider program of professionally led and adequately resourced change efforts, such guidelines will lack meaning, legitimacy, and authority among intended users and may be strongly resisted.
基于分子途径的“精准医学”的承诺,由于复杂的原因,对许多疾病仍然没有实现。临床实践指南(理论上)可以作为“开拓者”,引入反映精准医学发现的测试和治疗方法。我们描述了来自英国的一个详细案例研究,在该案例中,这种尝试(到目前为止)是不成功的,并展示了这种情况如何提供可推广的经验教训。政策制定者应该警惕仅将临床实践指南用作引入精准医学的唯一手段,甚至是主要手段。
精准医学针对疾病的潜在分子机制,取决于测量特定生物标志物的新技术,这些技术有望实现更准确的诊断、患者分层和量身定制的治疗。这些技术可能具有颠覆性——也就是说,它们使临床实践和服务组织的彻底变革成为可能,并且通常需要进行这种变革,从而提高护理质量、安全性或效率。临床实践指南可以作为“开拓者”,引入和使新的技术和实践合法化。
我们描述了一个案例研究,即学术研究人员试图使用便携式呼吸设备测量的精准医学生物标志物(呼出气一氧化氮分数,FeNO)彻底改变英国的哮喘管理。我们收集了一个广泛的数据集,其中包括 100 多个文件、61 次访谈和 150 小时的民族志观察,并使用技术增强的强结构理论(TESST)对其进行了分析。
我们的研究描述了呼吸医学学术研究人员为使用政府支持的国家指南为哮喘的精准医学方法铺平道路而进行的一次迄今为止不成功的尝试。这些研究人员认为,哮喘管理,尤其是在初级保健中,存在过度诊断和治疗方案不佳的问题;他们让国家指南制定机构参与努力解决这个问题;并确保该指南要求初级保健临床医生使用 FeNO 技术进行诊断和监测。然而,在没有更广泛的专业领导和充足资源的变革努力的情况下,在三级转诊中心之外工作的临床医生并没有接受或同意实施该指南中所体现的精准医学愿景——原因是多方面的,包括专业、操作和经济方面的原因。
只有在感兴趣的个人和团体中,推荐新技术的“开拓者”指南才可能在有限的范围内成功成为变革的催化剂。在缺乏更广泛的专业领导和充足资源的变革努力的情况下,这些指南将在预期用户中缺乏意义、合法性和权威性,并且可能会受到强烈抵制。